Evidence map›Paper›PMID 39677479›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Efficient multi-phenotype genome-wide analysis identifies genetic associations for unsupervised deep-learning-derived high-dimensional brain imaging phenotypes.

Bohong Guo, Ziqian Xie, Wei He, Sheikh Muhammad Saiful Islam, Assaf Gottlieb, Han Chen, Degui Zhi

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Bohong GuoDepartment of Biostatistics & Data Science, School of Public Health, University of Texas Health Science Center, Houston, Texas 77030, USA.ORCID 0000-0003-4595-912X
Ziqian XieDepartment of Bioinformatics and Systems Medicine, McWilliams School of Biomedical Informatics, University of Texas Health Science Center, Houston, Texas 77030, USA.
Wei HeDepartment of Bioinformatics and Systems Medicine, McWilliams School of Biomedical Informatics, University of Texas Health Science Center, Houston, Texas 77030, USA.
Sheikh Muhammad Saiful IslamDepartment of Bioinformatics and Systems Medicine, McWilliams School of Biomedical Informatics, University of Texas Health Science Center, Houston, Texas 77030, USA.
Assaf GottliebDepartment of Bioinformatics and Systems Medicine, McWilliams School of Biomedical Informatics, University of Texas Health Science Center, Houston, Texas 77030, USA.ORCID 0000-0003-4904-631X
Han ChenHuman Genetics Center, Department of Epidemiology, School of Public Health, The University of Texas Health Science Center at Houston, Houston, Texas 77030, USA.ORCID 0000-0002-9510-4923
Degui ZhiDepartment of Bioinformatics and Systems Medicine, McWilliams School of Biomedical Informatics, University of Texas Health Science Center, Houston, Texas 77030, USA.ORCID 0000-0001-7754-1890

Funding

Genetics of deep-learning-derived neuroimaging endophenotypes for Alzheimer's Disease (Parent grant)U01AG070112 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FORNAGE, MYRIAM, JI, SHUIWANG · 2021 to 2025
$7.2M
NIA NIH HHS U01 AG070112
6 · The paper itself

Abstract

Brain imaging is a high-content modality that offers dense insights into the structure and pathology of the brain. Existing genetic association studies of brain imaging, typically focusing on a number of individual image-derived phenotypes (IDPs), have successfully identified many genetic loci. Previously, we have created a 128-dimensional Unsupervised Deep learning derived Imaging Phenotypes (UDIPs), and identified multiple loci from single-phenotype genome-wide association studies (GWAS) for individual UDIP dimensions, using data from the UK Biobank (UKB). However, this approach may miss genetic associations where one single nucleotide polymorphism (SNP) is moderately associated with multiple UDIP dimensions. Here, we present Joint Analysis of multi-phenotype GWAS (JAGWAS), a new tool that can efficiently calculate multivariate association statistics using single-phenotype summary statistics for hundreds of phenotypes. When applied to UDIPs of T1 and T2 brain magnetic resonance imaging (MRI) on discovery and replication cohorts from the UKB, JAGWAS identified 195/168 independently replicated genomic loci for T1/T2, 6 times more than those from the single-phenotype GWAS. The replicated loci were mapped into 555/494 genes, and 217/188 genes overlapped with the expression quantitative trait loci (eQTL) of brain tissues. Gene enrichment analysis indicated that the genes mapped are closely related to neurobiological functions. Our results suggested that multi-phenotype GWAS is a powerful approach for genetic discovery using high-dimensional UDIPs.

Indexed as

EndophenotypeGWASImage-derived phenotypesImaging geneticsMultivariateStatistical genetics

Identifiers

PMID39677479
PMCPMC11643246

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.